4-5

Having Injectable Experience of Analytical Method Validation for Assay, Related Substances Content by HPLC and Residual Solvents by CC, Preparation and Review of Method Validation and Method Equivalency and Method Transfer Protocols and Reports.

Supervise production lines, including Granulation, Compression, Coating, and Packing. Good verbal and written English communication skills

Hands on Experience on, Stability Studies, Analytical Method Validation & Finished Goods.

Experience in review of HPLC, GC, LCMS calibration data & Analytical Data review &Review of Analytical Method Validations, Method Transfers, Protocols & Reports.

Able to perform Biochemical techniques, Chromatography techniques, Electrophoresis techniques, Immuno assay techniques, Cell culture techniques and Molecular techniques

Drive process improvements and system enhancements to optimize the use of Veeva Vault for Quality Management. Support the implementation and ongoing maintenance of Veeva Vault Quality modules aligned with regulatory and business needs.

Ciron has carved a niche for itself in the sphere of operations of manufacturing Ampoules, Vials, Eye / Ear / Nasal drops, Lyophilized products and Lyophilized bulk.

QMS Activities, Deviation, Change Control, Market Compliance, IPQA, Review of BMR & BPR, Lab QA, Exposure in OSD & Sterile

This is a non-supervisory position in Reference Standard Laboratory responsible for performing the required tests as part of the project and maintaining the GLP environment in the Laboratory.